1-Chlorohexane
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| Names | |
|---|---|
| Other names
1-Hexyl chloride
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| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.008.054 |
| EC Number |
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PubChem CID
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| UNII | |
| UN number | 1993 |
CompTox Dashboard (EPA)
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| Properties | |
| C6H13Cl | |
| Molar mass | 120.62 g·mol−1 |
| Appearance | Liquid |
| Density | 0.88 g/cm3 |
| Melting point | −94.0 °C (−137.2 °F; 179.2 K) |
| Boiling point | 135 °C (275 °F; 408 K) |
| sparingly soluble | |
| Hazards | |
| GHS labelling:[1] | |
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| Warning | |
| H226, H412 | |
| P210, P233, P240, P241, P242, P243, P273, P280, P303 P361 P353, P370 P378, P403 P235, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1-Chlorohexane is a chemical compound from the group of aliphatic saturated halogenated hydrocarbons. The chemical formula is CH3(CH2)5Cl.[2][3]
Synthesis
[edit]1-Chlorohexane can be obtained by reacting hexyl alcohol with hydrochloric acid or thionyl chloride.
Physical properties
[edit]1-Chlorohexane is a colorless liquid with an aromatic odor that is very sparingly soluble in water.[4]
Chemical properties
[edit]1-Fluorohexane can be prepared by reacting 1-chlorohexane with potassium fluoride in ethylene glycol.
2-Phenylhexane can be prepared by reacting the compound with benzene and aluminum trichloride.[5]
See also
[edit]References
[edit]- ^ "1-Chlorohexane". pubchem.ncbi.nlm.nih.gov.
- ^ "1-Chlorohexane". Sigma Aldrich. Retrieved 7 August 2024.
- ^ "Hexane, 1-chloro-". NIST. Retrieved 7 August 2024.
- ^ Lide, David R. (1993). CRC Handbook of Chemistry and Physics/Special Student Edition 1993-1994. CRC Press . p. 3-112. ISBN 978-0849305955. Retrieved 7 August 2024.
- ^ Fox, Scott (2004). Organic Chemistry. Jones and Bartlett Publishers. p. 530. ISBN 978-0763721978. Retrieved 7 August 2024.